Newer Therapeutic Approaches in Treating Alzheimer's Disease: A Comprehensive Review.

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-02-03 eCollection Date: 2025-02-18 DOI:10.1021/acsomega.4c05527
Radhakrishna Reddi Sree, Manjunath Kalyan, Nikhilesh Anand, Sangeetha Mani, Vasavi Rakesh Gorantla, Meena Kishore Sakharkar, Byoung-Joon Song, Saravana Babu Chidambaram
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Abstract

Alzheimer's disease (AD) is an aging-related irreversible neurodegenerative disease affecting mostly the elderly population. The main pathological features of AD are the extracellular Aβ plaques generated by APP cleavage through the amyloidogenic pathway, the intracellular neurofibrillary tangles (NFT) resulting from the hyperphosphorylated tau proteins, and cholinergic neurodegeneration. However, the actual causes of AD are unknown, but several studies suggest hereditary mutations in PSEN1 and -2, APOE4, APP, and the TAU genes are the major perpetrators. In order to understand the etiology and pathogenesis of AD, various hypotheses are proposed. These include the following hypotheses: amyloid accumulation, tauopathy, inflammation, oxidative stress, mitochondrial dysfunction, glutamate/excitotoxicity, cholinergic deficiency, and gut dysbiosis. Currently approved therapeutic interventions are donepezil, galantamine, and rivastigmine, which are cholinesterase inhibitors (ChEIs), and memantine, which is an N-methyl-d-aspartate (NMDA) antagonist. These treatment strategies focus on only symptomatic management of AD by attenuating symptoms but not regeneration of neurons or clearance of Aβ plaques and hyperphosphorylated Tau. This review focuses on the pathophysiology, novel therapeutic targets, and disease-altering treatments such as α-secretase modulators, active immunotherapy, passive immunotherapy, natural antioxidant products, nanomaterials, antiamyloid therapy, tau aggregation inhibitors, transplantation of fecal microbiota or stem cells, and microtubule stabilizers that are in clinical trials or still under investigation.

治疗阿尔茨海默病的新治疗方法:综合综述。
阿尔茨海默病(AD)是一种与年龄有关的不可逆神经退行性疾病,主要影响老年人。AD的主要病理特征是淀粉样蛋白途径APP裂解产生的细胞外Aβ斑块、tau蛋白过度磷酸化导致的细胞内神经原纤维缠结(NFT)和胆碱能性神经变性。然而,阿尔茨海默病的实际原因尚不清楚,但一些研究表明PSEN1和-2、APOE4、APP和TAU基因的遗传突变是主要的肇事基因。为了了解AD的病因和发病机制,人们提出了各种假说。这些假设包括:淀粉样蛋白积累、牛头病、炎症、氧化应激、线粒体功能障碍、谷氨酸/兴奋性毒性、胆碱能缺乏和肠道生态失调。目前批准的治疗干预措施是多奈哌齐、加兰他敏和利瓦斯汀,它们都是胆碱酯酶抑制剂(ChEIs),而美金刚是一种n -甲基-d-天冬氨酸(NMDA)拮抗剂。这些治疗策略仅侧重于通过减轻症状来对症管理AD,而不是神经元再生或清除Aβ斑块和过度磷酸化的Tau。本文综述了α-分泌酶调节剂、主动免疫疗法、被动免疫疗法、天然抗氧化剂、纳米材料、抗淀粉样蛋白疗法、tau聚集抑制剂、粪便微生物群或干细胞移植、微管稳定剂等临床试验或仍在研究中的病理生理学、新的治疗靶点和改变疾病的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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